RecallRadar

FDA Device recall Z-3208-2017

IMPRESSION CAP CONT 3.5MM, REF ZOCIMP3A

On 2017-10-04 the FDA classified a Class II recall of IMPRESSION CAP CONT 3.5MM, REF ZOCIMP3A by Zimmer Dental, citing zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard IFUs. All the produ….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-3208-2017
ClassificationClass II
Statusterminated
Initiated2017-07-10
Published2017-10-04
Last updated2026-09-13 11:54 UTC
CompanyZimmer Dental
Distributionn/a

Product

IMPRESSION CAP CONT 3.5MM, REF ZOCIMP3A; MPRESSION CAP CONT 3.5MM, REF ZOCIMP3S; IMPRESSION CAP CONT 4.5MM ANG, REF ZOCIMP4A; IMPRESSION CAP CONT 4.5MM, REF ZOCIMP4S; IMPRESSION CAP,CONT,5.5MM, ANG, REF ZOCIMP5A; IMPRESSION CAP, CONT, 5.5MM, REF ZOCIMP5S; MPRESSION CAP, CONT, 6.5MM,ANG, REF ZOCIMP6A; IMPRESSION CAP, CONT, 6.5MM, REF ZOCIMP6S

Reason

Zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard IFUs. All the products were missing supplemental IFUs.

Identifiers

code_infolot # 63275811, 63238369, 63286562, 63240994, 63250273, 63286560, 62556219, 62607124, 62675252, 62445681, 62086170, 62679151, 62734003

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3208-2017%22

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